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Female reproductive fluids ‘rescue’ sperm from phenotypic ageing in an external fertilizer

Female reproductive fluids (FRFs) serve key reproductive functions in sexually reproducing animals, including modifying the way sperm swim and detect eggs, and influencing sperm lifespan. Despite the central role of FRF during fertilization, we know surprisingly little about sperm–FRF interactions u...

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Detalles Bibliográficos
Autores principales: Hadlow, Jessica H., Evans, Jonathan P., Lymbery, Rowan A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10206448/
https://www.ncbi.nlm.nih.gov/pubmed/37221848
http://dx.doi.org/10.1098/rspb.2023.0574
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author Hadlow, Jessica H.
Evans, Jonathan P.
Lymbery, Rowan A.
author_facet Hadlow, Jessica H.
Evans, Jonathan P.
Lymbery, Rowan A.
author_sort Hadlow, Jessica H.
collection PubMed
description Female reproductive fluids (FRFs) serve key reproductive functions in sexually reproducing animals, including modifying the way sperm swim and detect eggs, and influencing sperm lifespan. Despite the central role of FRF during fertilization, we know surprisingly little about sperm–FRF interactions under different environmental conditions. Theory suggests that in external fertilizers FRF may ‘rescue’ sperm from ageing effects as they search to fertilize eggs. Here, we test the interaction between these two fundamental properties of the fertilization environment, ejaculate age (i.e. time since ejaculation) and FRF, on a range of functional sperm phenotypes in a broadcast spawning mussel, Mytilus galloprovincialis. We found that the effects of ejaculate age on multivariate sperm motility traits and total sperm motility were altered by FRF, and that longer-lived sperm exhibit stronger, likely more advantageous, responses to FRF after periods of ageing. We also detected significant among-male variation in the relationship between sperm motility traits and ejaculate age; notably, these patterns were only revealed when sperm encountered FRF. Collectively these findings underscore the importance of considering female reproductive physiology when interpreting ageing-related declines in sperm motility, as doing so may expose importance sources of variation in sperm phenotypic plasticity among males and environments.
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spelling pubmed-102064482023-05-25 Female reproductive fluids ‘rescue’ sperm from phenotypic ageing in an external fertilizer Hadlow, Jessica H. Evans, Jonathan P. Lymbery, Rowan A. Proc Biol Sci Behaviour Female reproductive fluids (FRFs) serve key reproductive functions in sexually reproducing animals, including modifying the way sperm swim and detect eggs, and influencing sperm lifespan. Despite the central role of FRF during fertilization, we know surprisingly little about sperm–FRF interactions under different environmental conditions. Theory suggests that in external fertilizers FRF may ‘rescue’ sperm from ageing effects as they search to fertilize eggs. Here, we test the interaction between these two fundamental properties of the fertilization environment, ejaculate age (i.e. time since ejaculation) and FRF, on a range of functional sperm phenotypes in a broadcast spawning mussel, Mytilus galloprovincialis. We found that the effects of ejaculate age on multivariate sperm motility traits and total sperm motility were altered by FRF, and that longer-lived sperm exhibit stronger, likely more advantageous, responses to FRF after periods of ageing. We also detected significant among-male variation in the relationship between sperm motility traits and ejaculate age; notably, these patterns were only revealed when sperm encountered FRF. Collectively these findings underscore the importance of considering female reproductive physiology when interpreting ageing-related declines in sperm motility, as doing so may expose importance sources of variation in sperm phenotypic plasticity among males and environments. The Royal Society 2023-05-31 2023-05-24 /pmc/articles/PMC10206448/ /pubmed/37221848 http://dx.doi.org/10.1098/rspb.2023.0574 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Behaviour
Hadlow, Jessica H.
Evans, Jonathan P.
Lymbery, Rowan A.
Female reproductive fluids ‘rescue’ sperm from phenotypic ageing in an external fertilizer
title Female reproductive fluids ‘rescue’ sperm from phenotypic ageing in an external fertilizer
title_full Female reproductive fluids ‘rescue’ sperm from phenotypic ageing in an external fertilizer
title_fullStr Female reproductive fluids ‘rescue’ sperm from phenotypic ageing in an external fertilizer
title_full_unstemmed Female reproductive fluids ‘rescue’ sperm from phenotypic ageing in an external fertilizer
title_short Female reproductive fluids ‘rescue’ sperm from phenotypic ageing in an external fertilizer
title_sort female reproductive fluids ‘rescue’ sperm from phenotypic ageing in an external fertilizer
topic Behaviour
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10206448/
https://www.ncbi.nlm.nih.gov/pubmed/37221848
http://dx.doi.org/10.1098/rspb.2023.0574
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